NDC 75568-024 - Dr. Scholls Blister Pain Relief Complete
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 75568-024
- Package NDCs from labels
- 75568-024-01
- Manufacturer
- Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd.
- Effective date
- 2024-12-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dr. Scholl's Blister Pain Relief Complete Kit | Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd. | 2024-12-18 | HUMAN OTC DRUG LABEL |
| Dr. Scholl's Blister Pain Relief Complete Kit | Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd. | 2024-12-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75568-024-01 | Dr. Scholls Blister Pain Relief Complete | 0.37 g in 1 PATCH | PATCH | 2.96 g | 40 mg in 1g | 2 |
| 75568-024-01 | Dr. Scholls Blister Pain Relief Complete | 0.37 g in 1 PATCH | PATCH | 4.44 g | 40 mg in 1g | 2 |
| 75568-024-01 | Dr. Scholls Blister Pain Relief Complete | 1 in 1 POUCH | PATCH | 40 mg in 1g | 2 | |
| 75568-024-01 | Dr. Scholls Blister Pain Relief Complete | 1 in 1 POUCH | PATCH | 40 mg in 1g | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 75568-024 | DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC] | 2 | Unmatched | 20250216_26e3a678-b28f-588b-e063-6394a90ac025.zip |
| 75568-024 | DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC] | 2 | Unmatched | 20250216_d860b339-48a0-405c-a67d-f7e7a31f6351.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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|---|---|---|---|---|---|---|
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| Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 8N Neutral | OCTISALATE, TITANIUM DIOXIDE | Parfums Christian Dior | b24806b1-d9da-4373-b072-6d9a262ea365 | 2026-05-06 | Warnings | 15FIX9V2JP |
| Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 5N Neutral | OCTISALATE, TITANIUM DIOXIDE | Parfums Christian Dior | c981ae5e-e7e8-484b-b682-fb96d501e03b | 2026-05-06 | Warnings | 15FIX9V2JP |
| CAREALL Hydrocortisone Maximum Strength | HYDROCORTISONE | New World Imports, Inc. | 5114cdba-96a1-c399-e063-6294a90aac12 | 2026-05-06 | Warnings | M017 |
| PREMIUM BEAUTY BALM BROAD SPECTRUM SPF 30 | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AND ZINC OXIDE | Have & Be Co., Ltd. | 4a7e868d-6310-6ee4-e063-6394a90aebce | 2026-05-06 | Warnings | 15FIX9V2JP |
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| Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 1W Warm | OCTISALATE, TITANIUM DIOXIDE | Parfums Christian Dior | 53a79ee7-312b-49a2-8a9b-c50794fcd171 | 2026-05-05 | Warnings | 15FIX9V2JP |
| Terocin | LIDOCAINE, MENTHOL | ASCLEMED USA INC. | 449ff436-a7d0-4f19-99af-4aa485a7f074 | 2026-05-05 | Warnings | 98PI200987 |
| New Terocin | METHYL SALICYLATE, CAPSAICIN, AND MENTHOL | ASCLEMED USA INC. | 68dc0231-3364-448b-bde9-f19fa122c765 | 2026-05-05 | Warnings | M017 |
| Glycerin | GLYCERIN SUPPOSITORIES | Neilmed Pharmaceuticals Inc. | 374a2ca3-ee04-09a7-e063-6394a90ab760 | 2026-05-05 | Warnings | PDC6A3C0OX |
| Neutrogena MINERAL UV TINT FACE DEEP SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Port Jervis Laboratories, Inc | 51169bed-2091-ad2b-e063-6294a90a84b6 | 2026-05-05 | Warnings | 15FIX9V2JP |
| Lidocaine 4% Patch | LIDOCAINE 4% | SOLA Pharmaceuticals | c31957dd-edea-ce98-e053-2a95a90a9c2d | 2026-05-05 | Warnings | M017 1737778 98PI200987 |
| Biofreeze Triple Target Gel | CAMPHOR, CAPSAICIN, MENTHOL | Reckitt Benckiser LLC | 511852c8-7428-3234-e063-6394a90a5bc2 | 2026-05-05 | Warnings | M017 |
| LUMINOUS EYE CORRECTOR SPF 41 - FAIR | TITANIUM DIOXIDE, ZINC OXIDE | Drmtlgy, LLC | 8cfb1f8c-1bd7-4983-ab82-1c9bd8925afa | 2026-05-04 | Warnings | 15FIX9V2JP |
| LUMINOUS EYE CORRECTOR SPF 41 - DEEP | TITANIUM DIOXIDE, ZINC OXIDE | Drmtlgy, LLC | 930bd1de-5a0e-4607-8d3c-b1ca918f890b | 2026-05-04 | Warnings | 15FIX9V2JP |
| 5Kind DMSO Pain Relieving | CAMPHOR (SYNTHETIC) | 5Kind Trading LTD | 62b55114-47f4-473a-8406-78238c3c1fa2 | 2026-05-04 | Warnings | M017 |
| Lidothol ES | MENTHOL 5%, LIDOCAINE 4% | Clinic Pharma | b456b63b-cead-4bed-aa2e-881fe88a77dc | 2026-05-04 | Warnings, Adverse reactions | 98PI200987 |
| Zinc Oxide with Menthol and White Petrolatum | MENTHOL, ZINC OXIDE, WHITE PETROLATUM | Aldermed Inc. | f993fc0a-bd80-4345-a948-65ac03f910e2 | 2026-05-04 | Warnings | M017 |
| EVERLIT CARE PRODUCTS BURN RELIEF | LIDOCAINE HYDROCHLORIDE | EVERLIT GLOBAL INC. | d7ec5720-4d1f-4943-ae36-c7d6acbae7d7 | 2026-05-04 | Warnings | M017 |
| EVERLIT CARE PRODUCTS BURN RELIEF | LIDOCAINE HYDROCHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | 5371dae4-ea63-46cc-ac26-5418f359c63e | 2026-05-04 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.